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Issue 5, 1995
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A diarylheptanoid intermediate in the biosynthesis of phenylphenalenones in Anigozanthos preissii

Abstract

The incorporation of 1-phenyl-7-(3,4-dihydroxyphenyl)hepta-1,3-dien-5-one and two molecules of cinnamic acid, respectively, into anigorufone by cultured roots of Anigozanthos preissii provides the first experimental evidence for the biosynthesis of a phenylphenalenone from two C6–C3 units via an open chain type diarylheptanoid.

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Article type: Paper
DOI: 10.1039/C39950000525
Citation: J. Chem. Soc., Chem. Commun., 1995,0, 525-526
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    A diarylheptanoid intermediate in the biosynthesis of phenylphenalenones in Anigozanthos preissii

    D. Hölscher and B. Schneider, J. Chem. Soc., Chem. Commun., 1995, 0, 525
    DOI: 10.1039/C39950000525

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